CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 591 enrolled
Drug / intervention
Mepolizumab 300 mgbiological
Likely dose
Mepolizumab 300 mgfrom record
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Search/NCT07591753
NCT07591753N/ACompleted

Assessing The Long-Term Effectiveness and Safety of Mepolizumab 300mg/Month in the European Real-Life Setting (Mepo Long-term Study)

European EGPA Study Group·observational·Posted May 18, 2026·Updated May 18, 2026

In Brief

An observational study evaluating Mepolizumab 300 mg for Eosinophilic Granulomatosis With Polyangiitis (Churg-Strauss) (EGPA). Completed, enrolled 591 participants across 1 site.

Detailed Summary

This observational study aims to evaluate the long-term effectiveness and safety of mepolizumab 300 mg/4 weeks in adults with eosinophilic granulomatosis with polyangiitis (EGPA) in the European real-life setting. The main questions it aims to answer are: * How effective is mepolizumab 300 mg/4 weeks over long-term follow-up in patients with EGPA? * How safe is mepolizumab 300 mg/4 weeks during long-term treatment? * What are the effects of switching mepolizumab dosage from 300 mg/4 weeks to 100 mg/4 weeks, or from 100 mg/4 weeks to 300 mg/4 weeks? Participants already receiving mepolizumab as part of routine clinical practice. Researchers will retrospectively collect demographic, clinical, laboratory, and treatment-related data from medical records. For patients starting mepolizumab 300 mg/4 weeks, data will be collected from treatment initiation and during follow-up up to 60 months. For patients who change mepolizumab dose, data will also be collected at the time of dose switch and 3 months later.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesItaly
CollaboratorsGlaxoSmithKline

Timeline

N/ACompletedFinished
2026
First PostedMay 18, 2026
Enrollment StartSep 18, 2025
Primary CompletionMar 31, 2026
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 1 month ago

Interventions

Mepolizumab 300 mgbiological

Mepolizumab administered subcutaneously at a dose of 300 mg every 4 weeks in routine clinical practice for adult patients with eosinophilic granulomatosis with polyangiitis (EGPA). In this retrospective observational study, patients may receive mepolizumab 300 mg/4 weeks as the initial regimen or after dose escalation from 100 mg/4 weeks. Dose changes from 300 mg/4 weeks to 100 mg/4 weeks, or from 100 mg/4 weeks to 300 mg/4 weeks, are also evaluated when they occur during routine care; no study-specific treatment is assigned.